Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

schaerer® arcus 501 — Class I MDR by Schaerer Medical AG

MD Atlas
Schaerer Medical AG

EUDAMED last updated this device on Oct 16, 2023

schaerer® arcus 501

764014393ArcusRB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Schaerer Medical AG
UDI-DI code: 07640143932566
Reference / catalog number: 92226

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Schaerer Medical AG
SRN: CH-MF-000038078
Manufacturer status: Active

Market distribution

Primary placement in Netherlands; available across 1 country total.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: schaerer® arcus 501
UDI-DI code: 07640143932566
Basic UDI-DI: 764014393ArcusRB
Reference / catalog number: 92226
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: CrNi with side rails, 25 x 10 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011202OPERATING TABLES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

2-part Leg Plates schaerer® axis 350764014393Accessories45On the market Abdominal rest764014393Accessories45On the market Adapter for DORO basic unit764014393Accessories45On the market Adapter for DORO® basic unit764014393Accessories45On the market Adapter for lower leg surgery764014393Accessories45On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.